ENST00000397676.8:c.515T>A
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Leu172His
|
|
ENST00000397676.7:c.515T>A
(ALG3)
|
ENSP00000380793.3:p.Leu172His
|
|
ENST00000411922.5:c.*91T>A
(ALG3)
|
ENSP00000394917.1:n.*91T>A
|
|
ENST00000414845.5:c.337+180T>A
(ALG3)
|
|
|
ENST00000423996.5:c.*280T>A
(ALG3)
|
ENSP00000407011.1:n.*280T>A
|
|
ENST00000444495.1:c.2106+100581A>T
(EIF2B5)
|
ENSP00000409142.1:n.2106+100581A>T
|
|
ENST00000445626.6:c.371T>A
(ALG3)
|
ENSP00000402744.2:p.Leu124His
|
|
ENST00000446569.1:c.225T>A
(ALG3)
|
|
|
ENST00000455059.5:c.395T>A
(ALG3)
|
ENSP00000397613.1:p.Leu132His
|
|
ENST00000461415.5:n.488T>A
(ALG3)
|
|
|
ENST00000477959.1:n.55T>A
(ALG3)
|
|
|
ENST00000482048.1:n.504T>A
(ALG3)
|
|
|
ENST00000488976.5:n.400T>A
(ALG3)
|
|
|
NM_001006941.2:c.371T>A
(ALG3)
|
NP_001006942.1:p.Leu124His
|
|
NM_005787.5:c.515T>A
(ALG3)
|
NP_005778.1:p.Leu172His
|
|
NR_024533.1:n.446T>A
(ALG3)
|
|
|
NR_024534.1:n.509T>A
(ALG3)
|
|
|
XM_011512322.1:c.416T>A
(ALG3)
|
XP_011510624.1:p.Leu139His
|
|
XM_011512323.1:c.395T>A
(ALG3)
|
XP_011510625.1:p.Leu132His
|
|
XM_011512323.2:c.395T>A
(ALG3)
|
XP_011510625.1:p.Leu132His
|
|
XM_024453296.1:c.293T>A
(ALG3)
|
XP_024309064.1:p.Leu98His
|
|
NM_005787.6:c.515T>A
(ALG3)
MANE Select
|
NP_005778.1:p.Leu172His
|
|